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1 sition (MPT), and aristolochic acid (ArA), a phospholipase A2 inhibitor.
2 exposure to fatty acid-free BSA or cytosolic phospholipase A2 inhibitors.
3 nt of DARas with antioxidants or a cytosolic phospholipase A2 inhibitor also restores the wild-type p
6 the effects of a putative specific cytosolic phospholipase A2 inhibitor, arachidonyl trifluoromethyl
11 iac myocytes with urocortin, or the specific phospholipase A2 inhibitor bromoenol lactone, reduces th
12 ith 5 microm 12-epi-scalaradial, a secretory phospholipase A2 inhibitor, caused similar changes in ce
14 e ER relocation of endogenous GC proteins by phospholipase A2 inhibitors demonstrate that Golgi-ER cy
15 phospholipase A2 and lipoprotein-associated phospholipase A2 inhibitors hold promise for the reducti
21 des the rationale for the development of the phospholipase A2 inhibitors varespladib methyl and darap
22 logy of RoBo-1 is to the snake serum-derived phospholipase A2 inhibitors, which uniquely contain two
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